Beta-Lactam Allergy De-labeling in a Pediatric Hospital.

Q2 Medicine Journal of Pediatric Pharmacology and Therapeutics Pub Date : 2024-04-01 Epub Date: 2024-04-08 DOI:10.5863/1551-6776-29.2.169
Shawn Meehl, Christina Salathe, Chelsea Cooley, Alejandro Jordan-Villegas, Federico R Laham, Akshita Madala, Mallory Cowart
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Abstract

Objective: To assess the ability to de-label pediatric patients of their beta-lactam allergy by using a newly implemented institutional protocol and to identify potential barriers to the de-labeling process.

Methods: All patients with reported allergies to prespecified beta-lactam antibiotics were eligible for a -beta-lactam allergy interview. Following the interview, patients were grouped into 4 risk categories-no risk, low risk, moderate risk, and high risk-and assessed for intervention eligibility. Potential interventions included de-labeling based on the interview alone or proceeding to an oral amoxicillin challenge with or without penicillin allergy skin testing.

Results: Of the 62 patients eligible for beta-lactam allergy interviews, 40% (n = 25) were de-labeled. Among de-labeled patients, 60% (n = 15) were de-labeled on the basis of the interview alone. Additionally, no failures were documented in patients who underwent an oral amoxicillin challenge or penicillin skin testing. Barriers to performing oral amoxicillin challenges or penicillin skin testing included concomitant systemic steroid or antihistamine use, refusal of intervention, and insufficient resources to perform penicillin skin testing.

Conclusions: There was a high frequency of patients de-labeled of their beta-lactam allergies in this study. Increased education to patients, parents, and providers on the de-labeling process, as well as increased personnel available to coordinate and perform de-labeling interventions, may result in more beta-lactam allergy de-labeling.

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一家儿科医院的β-内酰胺过敏去标签治疗
目的评估使用新实施的机构协议对β-内酰胺过敏的儿科患者进行去标签的能力,并找出去标签过程中可能存在的障碍:所有报告对预先指定的β-内酰胺类抗生素过敏的患者都有资格接受β-内酰胺过敏访谈。访谈结束后,患者被分为 4 个风险类别--无风险、低风险、中度风险和高风险--并进行干预资格评估。可能的干预措施包括仅根据面谈结果取消标签,或进行口服阿莫西林挑战,同时进行或不进行青霉素过敏皮试:在 62 名符合 beta-内酰胺过敏访谈条件的患者中,40%(n = 25)被取消标签。在被取消标签的患者中,60%(n = 15)仅凭面谈就被取消了标签。此外,在接受口服阿莫西林挑战或青霉素皮试的患者中,没有失败的记录。进行口服阿莫西林挑战或青霉素皮试的障碍包括同时使用全身类固醇或抗组胺药、拒绝干预以及没有足够的资源进行青霉素皮试:结论:在本研究中,患者对β-内酰胺类药物过敏而被取消标签的频率很高。加强对患者、家长和医疗服务提供者关于去标签过程的教育,以及增加协调和执行去标签干预的人员,可能会使更多的β-内酰胺过敏患者去标签。
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来源期刊
Journal of Pediatric Pharmacology and Therapeutics
Journal of Pediatric Pharmacology and Therapeutics Medicine-Pediatrics, Perinatology and Child Health
CiteScore
2.40
自引率
0.00%
发文量
90
期刊介绍: The Journal of Pediatric Pharmacology and Therapeutics is the official journal of the Pediatric Pharmacy Advocacy Group. JPPT is a peer-reviewed multi disciplinary journal that is devoted to promoting the safe and effective use of medications in infants and children. To this end, the journal publishes practical information for all practitioners who provide care to pediatric patients. Each issue includes review articles, original clinical investigations, case reports, editorials, and other information relevant to pediatric medication therapy. The Journal focuses all work on issues related to the practice of pediatric pharmacology and therapeutics. The scope of content includes pharmacotherapy, extemporaneous compounding, dosing, methods of medication administration, medication error prevention, and legislative issues. The Journal will contain original research, review articles, short subjects, case reports, clinical investigations, editorials, and news from such organizations as the Pediatric Pharmacy Advocacy Group, the FDA, the American Academy of Pediatrics, the American Society of Health-System Pharmacists, and so on.
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